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Treatment of Water Contaminated with Non-Steroidal Anti-Inflammatory Drugs Using Peroxymonosulfate Activated by Calcined Melamine@magnetite Nanoparticles Encapsulated into a Polymeric Matrix

In the present study, calcined melamine (CM) and magnetite nanoparticles (MNPs) were encapsulated in a calcium alginate (CA) matrix to effectively activate peroxymonosulfate (PMS) and generate free radical species for the degradation of ibuprofen (IBP) drug. According to the Langmuir isotherm model,...

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Autores principales: Darvishi Cheshmeh Soltani, Reza, Asgari, Fatemeh, Hassani, Negin, Yoon, Yeojoon, Khataee, Alireza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9698753/
https://www.ncbi.nlm.nih.gov/pubmed/36431944
http://dx.doi.org/10.3390/molecules27227845
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author Darvishi Cheshmeh Soltani, Reza
Asgari, Fatemeh
Hassani, Negin
Yoon, Yeojoon
Khataee, Alireza
author_facet Darvishi Cheshmeh Soltani, Reza
Asgari, Fatemeh
Hassani, Negin
Yoon, Yeojoon
Khataee, Alireza
author_sort Darvishi Cheshmeh Soltani, Reza
collection PubMed
description In the present study, calcined melamine (CM) and magnetite nanoparticles (MNPs) were encapsulated in a calcium alginate (CA) matrix to effectively activate peroxymonosulfate (PMS) and generate free radical species for the degradation of ibuprofen (IBP) drug. According to the Langmuir isotherm model, the adsorption capacities of the as-prepared microcapsules and their components were insignificant. The CM/MNPs/CA/PMS process caused the maximum degradation of IBP (62.4%) in 30 min, with a synergy factor of 5.24. Increasing the PMS concentration from 1 to 2 mM improved the degradation efficiency from 62.4 to 68.0%, respectively, while an increase to 3 mM caused a negligible effect on the reactor effectiveness. The process performance was enhanced by ultrasound (77.6% in 30 min), UV irradiation (91.6% in 30 min), and electrochemical process (100% in 20 min). The roles of [Formula: see text] and [Formula: see text] in the decomposition of IBP by the CM/MNPs/CA/PMS process were 28.0 and 25.4%, respectively. No more than 8% reduction in the degradation efficiency of IBP was observed after four experimental runs, accompanied by negligible leachate of microcapsule components. The bio-assessment results showed a notable reduction in the bio-toxicity during the treatment process based on the specific oxygen uptake rate (SOUR).
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spelling pubmed-96987532022-11-26 Treatment of Water Contaminated with Non-Steroidal Anti-Inflammatory Drugs Using Peroxymonosulfate Activated by Calcined Melamine@magnetite Nanoparticles Encapsulated into a Polymeric Matrix Darvishi Cheshmeh Soltani, Reza Asgari, Fatemeh Hassani, Negin Yoon, Yeojoon Khataee, Alireza Molecules Article In the present study, calcined melamine (CM) and magnetite nanoparticles (MNPs) were encapsulated in a calcium alginate (CA) matrix to effectively activate peroxymonosulfate (PMS) and generate free radical species for the degradation of ibuprofen (IBP) drug. According to the Langmuir isotherm model, the adsorption capacities of the as-prepared microcapsules and their components were insignificant. The CM/MNPs/CA/PMS process caused the maximum degradation of IBP (62.4%) in 30 min, with a synergy factor of 5.24. Increasing the PMS concentration from 1 to 2 mM improved the degradation efficiency from 62.4 to 68.0%, respectively, while an increase to 3 mM caused a negligible effect on the reactor effectiveness. The process performance was enhanced by ultrasound (77.6% in 30 min), UV irradiation (91.6% in 30 min), and electrochemical process (100% in 20 min). The roles of [Formula: see text] and [Formula: see text] in the decomposition of IBP by the CM/MNPs/CA/PMS process were 28.0 and 25.4%, respectively. No more than 8% reduction in the degradation efficiency of IBP was observed after four experimental runs, accompanied by negligible leachate of microcapsule components. The bio-assessment results showed a notable reduction in the bio-toxicity during the treatment process based on the specific oxygen uptake rate (SOUR). MDPI 2022-11-14 /pmc/articles/PMC9698753/ /pubmed/36431944 http://dx.doi.org/10.3390/molecules27227845 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Darvishi Cheshmeh Soltani, Reza
Asgari, Fatemeh
Hassani, Negin
Yoon, Yeojoon
Khataee, Alireza
Treatment of Water Contaminated with Non-Steroidal Anti-Inflammatory Drugs Using Peroxymonosulfate Activated by Calcined Melamine@magnetite Nanoparticles Encapsulated into a Polymeric Matrix
title Treatment of Water Contaminated with Non-Steroidal Anti-Inflammatory Drugs Using Peroxymonosulfate Activated by Calcined Melamine@magnetite Nanoparticles Encapsulated into a Polymeric Matrix
title_full Treatment of Water Contaminated with Non-Steroidal Anti-Inflammatory Drugs Using Peroxymonosulfate Activated by Calcined Melamine@magnetite Nanoparticles Encapsulated into a Polymeric Matrix
title_fullStr Treatment of Water Contaminated with Non-Steroidal Anti-Inflammatory Drugs Using Peroxymonosulfate Activated by Calcined Melamine@magnetite Nanoparticles Encapsulated into a Polymeric Matrix
title_full_unstemmed Treatment of Water Contaminated with Non-Steroidal Anti-Inflammatory Drugs Using Peroxymonosulfate Activated by Calcined Melamine@magnetite Nanoparticles Encapsulated into a Polymeric Matrix
title_short Treatment of Water Contaminated with Non-Steroidal Anti-Inflammatory Drugs Using Peroxymonosulfate Activated by Calcined Melamine@magnetite Nanoparticles Encapsulated into a Polymeric Matrix
title_sort treatment of water contaminated with non-steroidal anti-inflammatory drugs using peroxymonosulfate activated by calcined melamine@magnetite nanoparticles encapsulated into a polymeric matrix
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9698753/
https://www.ncbi.nlm.nih.gov/pubmed/36431944
http://dx.doi.org/10.3390/molecules27227845
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